Szok D, Hansen-Schwartz J, Edvinsson L
Department of Internal Medicine, Lund University Hospital, S-221 85 Lund, Sweden.
Neurosci Lett. 2001 Nov 13;314(1-2):69-72. doi: 10.1016/s0304-3940(01)02293-5.
Whereas the endothelin A receptor is generally believed to mediate vasoconstriction; the endothelin B receptor seems elusive; both dilative and constrictive responses have been reported. Using the in vitro arteriograph, a method allowing compartmentalized study of vessel segments, segments of rat middle cerebral artery were cannulated with micropipettes, pressurized and luminally perfused. Vessel diameters were evaluated using a microscope equipped with an imaging system. Both intra- and extraluminal applications of endothelin-1 produced constriction. Intraluminal administration of a selective endothelin B receptor agonist sarafotoxin 6c in precontracted cerebral arteries and in the presence of the endothelin A receptor blocker FR139317 caused vasodilation in a concentration-dependent manner. Inhibition of nitric oxide synthase significantly reduced the dilation induced by sarafotoxin 6c, whereas inhibition of cyclooxygenase and endothelium-derived hyperpolarizing factor did not.
一般认为内皮素A受体介导血管收缩;而内皮素B受体的作用似乎难以捉摸,有报道称其既有舒张反应又有收缩反应。使用体外动脉造影仪(一种可对血管段进行分区研究的方法),用微量移液器将大鼠大脑中动脉段插管,加压并进行腔内灌注。使用配备成像系统的显微镜评估血管直径。内皮素-1的腔内和腔外应用均引起收缩。在预先收缩的脑动脉中,在内皮素A受体阻滞剂FR139317存在的情况下,腔内给予选择性内皮素B受体激动剂沙拉毒素6c会引起浓度依赖性血管舒张。一氧化氮合酶的抑制显著降低了沙拉毒素6c诱导的舒张,而环氧合酶和内皮源性超极化因子的抑制则没有。